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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 21552Erstellt: 25. Oktober 2026

Benzyl Bromide → cis-4-Benzyloxy-2-buten-1-ol

https://huagongshe.com/reaction/21552

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBenzyl BromideHCID 7498—
Edukt2-Butene-1,4-diol, (2Z)-HCID 643790—
Produktcis-4-Benzyloxy-2-buten-1-olHCID 1100849263,2%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

14.6 g of sodium hydride (60 % in oil) was washed with n-pentane under an argon gas. After drying, 150 ml of dry dimethylformamide (hereinafter referred to simply as DMF) was added thereto to form a suspension. 75 g of (Z)-2-buten-1,4-diol was dropwise added thereto at 0° C. under stirring over a period of 30 minutes. The mixture was stirred at room temperature for 1.5 hours, and 44 g of benzyl bromide was added at 0° C. under stirring. The mixture was stirred at the same temperature for 30 minutes, and then the temperature was returned to room temperature. The mixture was stirred at 50° C. overnight. The reaction solution was poured into ice water and extracted with diethyl ether. The ether solution was washed sequentially with water and with a saturated sodium chloride aqueous solution and then dried over anhydrous magnesium sulfate. The solvent was distilled off under reduced pressure, and the residue was subjected to distillation under reduced pressure (2.5 mmHg, 134°-138° C.) to obtain 29 g of (Z)-4-benzyloxy-2-buten-1-ol as colorless oily substance.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05424309
Quelldatensatzuspto-grants-1995_06
ORD IDord-9186667cd3574337a99d237bd0b87c24
Quellennotizuspto-grants-1995_06